Canonical Allele Identifier: CA1076601618

Gene: ERCC8

Linked Data

• gnomAD v3: 5-60904674-A-ATC
• gnomAD v4: 5-60904674-A-ATC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904675_60904676insCT , CM000667.2:g.60904675_60904676insCT	GRCh38
NC_000005.9:g.60200502_60200503insCT , CM000667.1:g.60200502_60200503insCT	GRCh37
NC_000005.8:g.60236259_60236260insCT	NCBI36
NG_009289.1:g.45404_45405insGA , LRG_466:g.45404_45405insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.481+117_481+118insGA	ENSP00000408344.2:n.481+117_481+118insGA
ENST00000647431.2:c.582+117_582+118insGA	ENSP00000494726.2:n.582+117_582+118insGA
ENST00000647486.2:c.481+117_481+118insGA	ENSP00000494466.2:n.481+117_481+118insGA
ENST00000675042.2:c.307+117_307+118insGA	ENSP00000502082.2:n.307+117_307+118insGA
ENST00000675452.2:c.*446+117_*446+118insGA	ENSP00000506954.1:n.*446+117_*446+118insGA
ENST00000682217.1:c.481+117_481+118insGA	ENSP00000507570.1:n.481+117_481+118insGA
ENST00000682246.1:n.537+117_537+118insGA
ENST00000682375.1:c.*311+117_*311+118insGA	ENSP00000507551.1:n.*311+117_*311+118insGA
ENST00000683052.1:c.283+117_283+118insGA	ENSP00000507072.1:n.283+117_283+118insGA
ENST00000683199.1:n.503+117_503+118insGA
ENST00000683216.1:n.750+113_750+114insGA
ENST00000683460.1:c.*311+117_*311+118insGA	ENSP00000507820.1:n.*311+117_*311+118insGA
ENST00000684394.1:n.536+117_536+118insGA
ENST00000684453.1:n.531+117_531+118insGA
ENST00000684621.1:n.537+117_537+118insGA
ENST00000265038.10:c.481+117_481+118insGA	ENSP00000265038.6:n.481+117_481+118insGA
ENST00000497892.6:c.*279+117_*279+118insGA	ENSP00000501805.1:n.*279+117_*279+118insGA
ENST00000643034.1:c.*373+117_*373+118insGA	ENSP00000496080.1:n.*373+117_*373+118insGA
ENST00000643708.1:c.*311+117_*311+118insGA	ENSP00000494199.1:n.*311+117_*311+118insGA
ENST00000647431.1:c.533+117_533+118insGA
ENST00000647486.1:c.432+117_432+118insGA
ENST00000675042.1:c.307+117_307+118insGA	ENSP00000502082.1:n.307+117_307+118insGA
ENST00000675229.1:c.481+117_481+118insGA	ENSP00000502154.1:n.481+117_481+118insGA
ENST00000675378.1:c.481+117_481+118insGA	ENSP00000502535.1:n.481+117_481+118insGA
ENST00000675452.1:n.730+117_730+118insGA
ENST00000675920.1:n.1089+117_1089+118insGA
ENST00000676185.1:c.481+117_481+118insGA MANE Select	ENSP00000501614.1:n.481+117_481+118insGA
ENST00000265038.9:c.481+117_481+118insGA	ENSP00000265038.5:n.481+117_481+118insGA
ENST00000381118.7:c.*525+117_*525+118insGA	ENSP00000370510.3:n.*525+117_*525+118insGA
ENST00000439176.5:c.307+117_307+118insGA	ENSP00000408344.1:n.307+117_307+118insGA
ENST00000462279.5:n.326+117_326+118insGA
ENST00000484330.5:n.227-2167_227-2166insGA
ENST00000495985.5:n.258+113_258+114insGA
ENST00000497892.5:n.524+117_524+118insGA
NM_000082.3:c.481+117_481+118insGA , LRG_466t1:c.481+117_481+118insGA	NP_000073.1:n.481+117_481+118insGA
NM_001007233.2:c.307+117_307+118insGA	NP_001007234.1:n.307+117_307+118insGA
NM_001007234.2:c.481+117_481+118insGA	NP_001007235.1:n.481+117_481+118insGA
NM_001290285.1:c.23-959_23-958insGA	NP_001277214.1:n.23-959_23-958insGA
NM_001007234.3:c.481+117_481+118insGA	NP_001007235.1:n.481+117_481+118insGA
NM_000082.4:c.481+117_481+118insGA MANE Select	NP_000073.1:n.481+117_481+118insGA
NM_001007233.3:c.307+117_307+118insGA	NP_001007234.1:n.307+117_307+118insGA
NM_001290285.2:c.23-959_23-958insGA	NP_001277214.1:n.23-959_23-958insGA